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- Ensaio Clínico NCT07819578
Toripalimab Plus Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable NSCLC
13 de setembro de 2026 atualizado por: Shaodong Hong
A Phase II Study of Toripalimab Combined With Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable Non-Small Cell Lung Cancer
This is a prospective, multicenter, single-arm Phase II investigator-initiated trial evaluating neoadjuvant toripalimab plus sacituzumab tirumotecan (SKB264) in treatment-naive adults with resectable or potentially resectable, driver-negative non-small cell lung cancer (NSCLC).
Eligible participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2) and will receive sacituzumab tirumotecan 5 mg/kg plus toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles.
Participants deemed operable after multidisciplinary assessment will undergo definitive surgery.
The primary endpoint is pathologic complete response.
A Simon two-stage minimax design plans to enroll 30 participants.
Visão geral do estudo
Status
Ainda não está recrutando
Condições
Intervenção / Tratamento
Descrição detalhada
This prospective, multicenter, single-arm Phase II investigator-initiated trial evaluates neoadjuvant sacituzumab tirumotecan (SKB264), a TROP2-directed antibody-drug conjugate, plus the PD-1 antibody toripalimab in treatment-naive adults with resectable or potentially resectable, driver-negative NSCLC.
Participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2).
Sacituzumab tirumotecan 5 mg/kg and toripalimab 3 mg/kg are administered intravenously on Day 1 every 2 weeks for up to 6 cycles.
Surgery is planned 4-6 weeks after the final neoadjuvant dose when the participant remains operable following multidisciplinary assessment.
Tumor response is assessed using RECIST 1.1.
Safety is assessed using NCI CTCAE version 5.0, including adverse events, serious adverse events, perioperative complications, and surgery delays or cancellations.
The primary endpoint is pathologic complete response, defined as no residual viable tumor cells in the resected primary tumor and all resected lymph nodes.
Major pathologic response is defined as residual viable tumor of 10% or less.
Tipo de estudo
Intervencional
Inscrição (Estimado)
30
Estágio
- Fase 2
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Contato de estudo
- Nome: Shaodong Hong Hong, M.D., Ph.D.
- Número de telefone: +8615920527656
- E-mail: hongshd@sysucc.org.cn
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Não
Descrição
Inclusion Criteria:
- Signed informed consent obtained before any study procedure.
- Age 18 to 75 years, male or female.
- Histologically/cytologically confirmed, treatment-naive, resectable or potentially resectable NSCLC: stage II-IIIA and selected IIIB (T3N2, T4N2) per IASLC/UICC TNM 9th edition.
- Disease staged as cTNM by PET-CT or by neck/chest/abdominal/pelvic CT plus whole-body bone scan and brain MRI.
- Multidisciplinary team including thoracic surgeon judges lesion resectable or potentially resectable.
- At least one measurable target lesion per RECIST 1.1.
- ECOG performance status 0-1.
- Adequate organ function (baseline, no transfusion, rh-EPO, or G-CSF within 2 weeks before first dose): neutrophils ≥1.5 ×10^9/L; platelets ≥100 ×10^9/L; hemoglobin ≥9 g/dL.
- AST, ALT, ALP ≤2.5 × ULN; TBil ≤1.5 × ULN.
- For liver metastases: AST/ALT ≤5 × ULN; TBil ≤2 × ULN.
- For liver or bone metastases: ALP ≤5 × ULN.
- Creatinine clearance (Cockcroft-Gault) ≥60 mL/min.
- INR, APTT, PT ≤1.5 × ULN.
- TSH within normal range; if TSH abnormal but T3 and free T4 normal, eligible.
- Women of childbearing potential must have a negative pregnancy test within 7 days before first dose and use effective contraception during treatment and until 12 months after last dose; men with partners of childbearing potential must use effective contraception during treatment and until 12 months after last dose.
Exclusion Criteria:
- Neuroendocrine histology component in tumor pathology.
- Known EGFR sensitizing mutation or ALK fusion (for non-squamous NSCLC, EGFR/ALK status must be determined).
- Other malignancy within 5 years, except those with clinically negligible metastatic risk and curative treatment intent (e.g., adequately treated carcinoma in situ as per protocol examples).
- Severe or uncontrolled comorbidities, including symptomatic cerebrovascular events or liver disease at Child-Pugh grade ≥A.
- History of allogeneic stem cell transplantation or solid organ transplantation.
- Severe dry eye syndrome, severe meibomian gland dysfunction, severe blepharitis, or corneal disorders that may delay corneal healing.
- History of interstitial lung disease requiring steroids, or active ILD.
- HIV positive or diagnosed AIDS.
- Active tuberculosis.
- Uncontrolled active HBV infection (HBsAg positive with HBV-DNA above local upper limit of normal). HBV-DNA must be <500 IU/mL within 28 days before randomization/inclusion.
- Active HCV infection (HCV antibody positive and HCV RNA positive).
- Known hypersensitivity to toripalimab or sacituzumab tirumotecan (or excipients).
- Live vaccine within 30 days before first dose (except inactivated vaccines allowed where specified by protocol, including local policy).
- Any systemic or local anticancer treatment before first study treatment.
- Use of traditional Chinese medicines with anticancer indication within 7 days before first dose, or need to continue such drugs during study.
- Other investigational drug not discontinued for at least 5 half-lives or 2 months (whichever is longer) before first dose.
- Any known or suspected autoimmune disease or immunodeficiency, except primary hypothyroidism (stable, not requiring hormones, or stable on physiologic hormone replacement) and stable type 1 diabetes mellitus with controlled blood glucose.
- Medical or psychiatric conditions likely to cause premature discontinuation or compromise safety, sampling, or follow-up, including severe social or compliance risks.
- Pregnancy or breastfeeding; unwillingness to use effective contraception as specified.
- Any other condition considered unsuitable by investigator.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Toripalimab plus sacituzumab tirumotecan
Participants will receive sacituzumab tirumotecan 5 mg/kg intravenously on Day 1 every 2 weeks combined with toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy.
Surgery will be performed after multidisciplinary assessment when appropriate.
Postoperative or adjuvant treatment will be determined according to guidelines and investigator assessment.
|
Toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with sacituzumab tirumotecan.
Sacituzumab tirumotecan (SKB264) 5 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with toripalimab.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Pathological Complete Response (pCR) Rate
Prazo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with no residual viable tumor cells in the resected primary tumor and all resected lymph nodes.
Participants without surgery or evaluable surgical pathology will be counted as non-pCR.
|
At definitive surgery, up to 18 weeks after first study treatment
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Major Pathological Response (MPR) Rate
Prazo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with residual viable tumor of 10% or less in the resected primary tumor and all resected lymph nodes.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
R0 Resection Rate
Prazo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants who undergo R0 resection, defined as microscopically margin-negative resection, after neoadjuvant therapy.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
Pathological Downstaging Rate
Prazo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with pathological stage lower than baseline clinical stage at definitive surgery.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
Objective Response Rate (ORR)
Prazo: Up to 18 weeks after first study treatment
|
Proportion of participants with complete response or partial response according to investigator-assessed RECIST 1.1 after neoadjuvant therapy.
|
Up to 18 weeks after first study treatment
|
|
Event-Free Survival (EFS)
Prazo: Up to 60 months from enrollment
|
Time from enrollment to disease progression precluding surgery, disease progression or recurrence after surgery, disease progression in participants who do not undergo surgery, or death from any cause, whichever occurs first.
|
Up to 60 months from enrollment
|
|
Overall Survival (OS)
Prazo: Up to 60 months from enrollment
|
Time from enrollment to death from any cause.
|
Up to 60 months from enrollment
|
|
Incidence of Adverse Events
Prazo: From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later
|
Incidence of adverse events graded according to NCI CTCAE version 5.0.
|
From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Estimado)
1 de outubro de 2026
Conclusão Primária (Estimado)
1 de dezembro de 2028
Conclusão do estudo (Estimado)
1 de dezembro de 2028
Datas de inscrição no estudo
Enviado pela primeira vez
24 de julho de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
13 de setembro de 2026
Primeira postagem (Real)
15 de setembro de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
15 de setembro de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
13 de setembro de 2026
Última verificação
1 de setembro de 2026
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 2026-FXY-019-NEIKE
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Descrição do plano IPD
De-identified individual participant data and data dictionaries from this investigator-initiated Phase II oncology study will not be shared at this time due to current sponsor/institutional policy, data governance requirements, and pending legal/ethics arrangements.
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .